Results 1 -
7
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7
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Cone dystrophy "1," "X-linked"
- ... LINKED, 3; CORDX3 CONE-ROD DYSTROPHY 6; CORD6 CONE-ROD DYSTROPHY, X-LINKED, 1; CORDX1 CONE-ROD DYSTROPHY 5; CORD5 CONE-ROD DYSTROPHY, X-LINKED, 2; CORDX2 CONE-ROD DYSTROPHY 7; CORD7 CONE- ...
- ... WITHOUT DEAFNESS; RPSRDF RETINITIS PIGMENTOSA GTPase REGULATOR; RPGR CONE-ROD DYSTROPHY, X-LINKED, 1; CORDX1 NCBI Gene ClinVar Ayyagari R, Demirci FY, ...
- ... J, Sankila EM, Alitalo T, Bech-Hansen NT. X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the ...
- ... conditions include autosomal recessive congenital stationary night blindness, X-linked congenital stationary night blindness, Stickler syndrome, Marfan syndrome, retinitis pigmentosa, cone-rod dystrophy, deafness and myopia syndrome, Knobloch syndrome, and Cohen ...
- ... present in other family members. Pigmentary retinopathy Rod-cone dystrophy RP Tapetoretinal degeneration Genetic Testing Registry: Retinitis pigmentosa ...
- ... OPN1SW Red-green color vision defects and blue cone monochromacy are inherited in an X-linked recessive pattern. The OPN1LW and OPN1MW genes are ... TR, Mollon JD, Moore AT, Hardcastle AJ. Blue cone monochromacy: causative mutations and ... Epub 2009 May 1. Citation on PubMed or Free article on PubMed ...
- Exercising with a Muscle Disease (Muscular Dystrophy Association) - PDFmuscular dystrophy; exercise with a disability; neuromuscular disease; adapted exercise; accesible sports equipment; power wheelchair; power soccer